Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,622 recalls have been distributed to New Jersey in the last 12 months.
Showing 35741–35760 of 53,621 recalls
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...
The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...
The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...
The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mentor MemoryGel Breast Implant Recalled by Mentor Texas, LP. Due to The box...
The Issue: The box of 300cc MemoryGel Breast Implant was labeled with null...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...
The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...
The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Huberts Lemonade Blackberry Recalled by Coca-Cola Company (The) Due to...
The Issue: The product may contain foreign material (glass) in some bottles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Huberts Lemonade Strawberry Recalled by Coca-Cola Company (The) Due to...
The Issue: The product may contain foreign material (glass) in some bottles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Huberts Lemonade Watermelon Recalled by Coca-Cola Company (The) Due to...
The Issue: The product may contain foreign material (glass) in some bottles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Huberts Original Lemonade Recalled by Coca-Cola Company (The) Due to Foreign...
The Issue: The product may contain foreign material (glass) in some bottles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...
The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...
The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection Recalled by...
The Issue: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.